number of ATP molecules produced during cellular respiration
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glycolysis
breaks glucose (C6) into 2 pyruvate (C3), located in cytoplasm
4
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citric acid cycle
breaks pyruvate into carbon dioxide, supplies next stage with electrons, located in mitochondria
5
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oxidative phosphorylation
electrons shuttled through ETC, ATP is generated in association with chemiosmosis, located in inner mitochondrial membrane
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steps of glycolysis
1-3) fuel molecule is energized using ATP 4) 6C intermediate splits into 2 3C intermediates 5) redox reaction generates NADH 6-9) ATP and pyruvate are produced (1-4 is energy investment, 5-9 is energy payoff)
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products of glycolysis
2 pyruvate, 2NADH, 2 net ATP (4ATP/2ADP), 2 water molecules leave
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steps of citric acid cycle
1) acetyl CoA brings 2 carbons into cycle 2-3) NADH, ATP, CO2 are generated during redox reactions, 4-5) redox reactions generate FADH2 and NADH
transfer of P group from substrate to ADP to produce ATP
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preparatory reaction
pyruvate is prepped in mitochondria to enter citric acid cycle (converted to acetyl CoA- 2 carbon molecule)
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fermentation
breaks down glucose without oxygen
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electron transport chain
pumps H+ ions, NAD+, FAD, releases water, ATP are made through ATP synthase (chemiosmosis), oxygen is the final acceptor
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how cellular poisons affect cellular respiration
1) blocks ETC 2) inhibits ATP synthase 3) makes the membrane leak H+ ions
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rotenone, cyanogenic glycosides
poisons that block ETC
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antibiotic oligomycin
poisons that inhibit ATP synthase
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dinitrophenol
poisons that make membrane leaky
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lactic acid fermentation
muscle cells and certain bacteria, makes 2 ATP/2NADH
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alcohol fermentation
baking and winemaking, makes CO2, NAD+
20
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cell cycle
ordered set of stages that takes place between time eukaryotic cell divides and the time resulting daughter cells also divide
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asexual reproduction
faster, don’t spend energy to find mate, little genetic diversity
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interphase
growth and DNA synthesis occur when nucleus is not actively dividing, cells spend 90% of time here
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chromatid
each double helix
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histones
group of proteins found in chromatin
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G1 phase
growth, increase in cytoplasm, DNA repair (# of organelles increases)
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S phase
DNA replication and growth
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G2 phase
growth, DNA repair, prep for division
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G1 checkpoint
checks DNA for damage to send to S phase, if damaged goes to G0 state
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G0
cells exit interphase, cells continue to perform normal processes with no prep for cell division, can reenter cycle if conditions become suitable for growth
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p53
protein that stops cycle if DNA is impossible to repair
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sister chromatids
formed during S phase, identical DNA molecules, joined at centromere
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centromere
region of chromosomes microtubule spindles attach via kinetochore
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G2 checkpoint
checks proper DNA replication to move to M
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mitosis
division of nucleus
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cytokinesis
division of cytoplasm
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M checkpoint
checks chromosome alignment
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apoptosis
programmed cell death, occurs if checkpoints detect errors
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hair cell
example of cell that passes through G1 checkpoint
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euchromatin
chromatin with lower level of compaction, accessible for transcription
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heterochromatin
highly compact chromatin not accessible for transcription
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prophase
formation of mitotic spindle, each centrosome has a pair of centrioles, chromosomes condense in nucleus, mitotic spindles elongate in cytoplasm
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prometaphase
nuclear envelope disappears, spindle microtubules reach chromosomes, microtubules attach to centromeres of sister chromatids at kinetochore, chromosomes moved to center of cell
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metaphase
spindle is fully formed, chromosomes align at cell equator (plate), kinetochores are facing opposite poles of spindle
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anaphase
chromatids are separate and move to opposite poles, motor proteins move chromosomes along spindle microtubules, microtubules attached to kinetochore shorten, cell elongates
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telophase
cell continues to elongate, nuclear membrane forms at each pole, chromosomes unfold and disperse, spindle microtubules disassemble
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cytokinesis in animal cells
cleavage furrow and contractile ring of actin and myosin microfilaments (pinches cell in 2) formed
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cytokinesis in plant cells
vesicles from Golgi apparatus form cell plate of cellulose and proteins, cell plate grows outward to reach edges which divides content into 2 cells each with plasma membrane and cell wall
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protooncogenes
promote cell cycle and prevent apoptosis, caused by mutations to oncogenes
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tumor suppressor genes
inhibit cell cycle, mutations inactivate genes which causes uncontrolled division
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somatic cells
body cells, pairs of homologous chromosomes, one from each parent
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homologous chromosomes
same length, centromere position, gene locations/locus (different versions of a gene at same locus)
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autosomes
all chromosomes that aren’t sex chromosomes (X/Y)
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meiosis
reduces number of chromosomes in half
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meiosis I
separates homologous chromosomes, chromosome # cut in half
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meiosis II
separates sister chromatids, chromosome # stays the same
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prophase I
chromosomes are compacted, synapsis occurs (homologous chromosomes attached by proteins), tetrads form (4 chromatids), non-sister chromosomes exchange genetic material (crossing over), spindle fibers form
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metaphase I
tetrads align at cell equator (plate), microtubules attach to kinetochore
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anaphase I
homologous pairs separate and move towards opposite poles
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telophase I
chromosomes move to poles with haploid set at each pole (linked sister chromatids, some form nuclear membrane around chromosomes), cytokinesis
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prophase II
chromosomes coil and compact, spindle apparatus forms and attaches to kinetochores of each sister chromatid
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metaphase II
duplicated chromosomes align at metaphase plate, kinetochores of sister chromatids face opposite poles
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anaphase II
centromeres of sister chromatids separate, chromatids move to opposite poles
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telophase II
chromosomes reach poles of cell, nuclear envelope forms, cytokinesis, 4 haploid daughter cells
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why offspring aren’t identical to parents
1) Independent orientation of chromosomes at metaphase I 2) random fertilization 3) different alleles on homologous genes 4) crossing over
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karyotype
picture of chromosomes dividing in cell
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nondisjunction
failure of chromosomes or chromatids to separate during meiosis
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aneuploidy
change in chromosome # resulting from nondisjunction during meiosis
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klinefelter syndrome
XXY male, most common,
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turner syndrome
X0 female, all or part of one sex chromosome is absent
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deletion
end of chromosome breaks off
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duplication
presences of chromosome segregation more than once in the same chromosome
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inversion
segment of chromosome is turned 180 degrees
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translocation
movement of chromosome segment from one chromosome to another non homologous chromosome (reciprocal if there is swapping between chromosomes)